Назад
Company hidden
8 дней назад

Project Manager I (Clinical Research)

65 000 - 75 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Project Manager I (Clinical Research): Managing a federally funded, five-year clinical research study with an accent on regulatory oversight, multi-site protocol implementation, participant coordination, and research data quality. Focus on maintaining human-subjects compliance, supervising study personnel, coordinating digital health assessments, and resolving operational issues across collaborating institutions.

Location: On-site in Tampa, Florida, United States

Salary: $65,000–$75,000 per year

Company

hirify.global is a public research university with extensive federally funded research activity and health sciences programs.

What you will do

  • Manage daily operations for a federally funded, five-year clinical research study.
  • Coordinate participant recruitment, screening, enrollment, informed consent, study visits, retention, and follow-up assessments.
  • Prepare and maintain IRB submissions, amendments, continuing reviews, adverse event reports, protocol deviations, and regulatory correspondence.
  • Implement study protocols across multiple research sites and oversee participant assessments, intervention delivery, data collection, and study supplies.
  • Maintain quality assurance and data quality procedures, prepare safety monitoring reports, and recommend process improvements.
  • Recruit, train, supervise, and evaluate research nurses, health coaches, student workers, research assistants, and volunteers.

Requirements

  • Bachelor’s degree in a related field and at least two years of project management or coordination experience; four years of direct experience may substitute for the degree.
  • Employment eligibility requirements in the United States must be met.
  • Knowledge of human-subjects research regulations, Good Clinical Practice, and Institutional Review Board processes.
  • Experience with project coordination, organization, leadership, communication, and multi-site collaboration.
  • Ability to manage regulatory documentation, participant safety, protocol fidelity, research data, and operational reporting.
  • Ability to work on-site in Tampa and supervise study personnel.

Nice to have

  • Master’s degree in Nursing, Public Health, Health Sciences, Exercise Science, Psychology, or a related health field.
  • Experience coordinating federally funded clinical, behavioral, or translational research studies.
  • Experience with cardiovascular disease populations, women’s health research, and studies from initiation through closeout.
  • ACRP, SOCRA, or equivalent professional research certification.
  • Experience with electronic health records, REDCap, and electronic data capture systems.

Culture & Benefits

  • Grant-funded, time-limited position with a contract of up to five years.
  • Medical, dental, and life insurance plans.
  • Retirement plan options and generous leave.
  • Employee and dependent tuition programs.
  • Additional employee perks and discounts.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →